Visual Discrimination, Serial Reversal, and Extinction Learning in the mdx Mouse

Duchenne muscular dystrophy (DMD) is the most common form of muscular dystrophy and the most common neuromuscular disorder. In addition to neuromuscular consequences, some individuals with DMD experience global intellectual dysfunction and executive dysfunction of unknown mechanistic origin. The cog...

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Main Authors: Price E. Dickson, Guy Mittleman
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-08-01
Series:Frontiers in Behavioral Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fnbeh.2019.00200/full
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spelling doaj-d6cb7df4265b4505bbc9fc0d7a1ade602020-11-24T21:22:23ZengFrontiers Media S.A.Frontiers in Behavioral Neuroscience1662-51532019-08-011310.3389/fnbeh.2019.00200473622Visual Discrimination, Serial Reversal, and Extinction Learning in the mdx MousePrice E. Dickson0Guy Mittleman1The Jackson Laboratory, Bar Harbor, ME, United StatesDepartment of Psychological Science, Ball State University, Muncie, IN, United StatesDuchenne muscular dystrophy (DMD) is the most common form of muscular dystrophy and the most common neuromuscular disorder. In addition to neuromuscular consequences, some individuals with DMD experience global intellectual dysfunction and executive dysfunction of unknown mechanistic origin. The cognitive profile of the mdx mouse, the most commonly used mouse model of DMD, has been incompletely characterized and has never been assessed using the touchscreen operant conditioning paradigm. The touchscreen paradigm allows the use of protocols that are virtually identical to those used in human cognitive testing and may, therefore, provide the most translational paradigm for quantifying mouse cognitive function. In the present study, we used the touchscreen paradigm to assess the effects of the mdx mutation on visual discrimination learning, serial reversal learning, and extinction learning. To enable measuring task-dependent learning and memory processes while holding demands on sensory-driven information processing constant, we developed equally salient visual stimuli and used them on all experimental stages. Acquisition of the initial pairwise visual discrimination was facilitated in mdx mice relative to wildtype littermates; this effect was not explained by genotypic differences in impulsivity, motivation, or motor deficits. The mdx mutation had no effect on serial reversal or extinction learning. Together, findings from this study and previous studies suggest that mdx effects on cognitive function are task-specific and may be influenced by discrimination type (spatial, visual), reward type (food, escape from a non-preferred environment), sex, and genetic background.https://www.frontiersin.org/article/10.3389/fnbeh.2019.00200/fullDuchenne muscular dystrophydystrophinC57BL/10ScSn-Dmdmdxoperant conditioningtouchscreenbehavioral flexibility
collection DOAJ
language English
format Article
sources DOAJ
author Price E. Dickson
Guy Mittleman
spellingShingle Price E. Dickson
Guy Mittleman
Visual Discrimination, Serial Reversal, and Extinction Learning in the mdx Mouse
Frontiers in Behavioral Neuroscience
Duchenne muscular dystrophy
dystrophin
C57BL/10ScSn-Dmdmdx
operant conditioning
touchscreen
behavioral flexibility
author_facet Price E. Dickson
Guy Mittleman
author_sort Price E. Dickson
title Visual Discrimination, Serial Reversal, and Extinction Learning in the mdx Mouse
title_short Visual Discrimination, Serial Reversal, and Extinction Learning in the mdx Mouse
title_full Visual Discrimination, Serial Reversal, and Extinction Learning in the mdx Mouse
title_fullStr Visual Discrimination, Serial Reversal, and Extinction Learning in the mdx Mouse
title_full_unstemmed Visual Discrimination, Serial Reversal, and Extinction Learning in the mdx Mouse
title_sort visual discrimination, serial reversal, and extinction learning in the mdx mouse
publisher Frontiers Media S.A.
series Frontiers in Behavioral Neuroscience
issn 1662-5153
publishDate 2019-08-01
description Duchenne muscular dystrophy (DMD) is the most common form of muscular dystrophy and the most common neuromuscular disorder. In addition to neuromuscular consequences, some individuals with DMD experience global intellectual dysfunction and executive dysfunction of unknown mechanistic origin. The cognitive profile of the mdx mouse, the most commonly used mouse model of DMD, has been incompletely characterized and has never been assessed using the touchscreen operant conditioning paradigm. The touchscreen paradigm allows the use of protocols that are virtually identical to those used in human cognitive testing and may, therefore, provide the most translational paradigm for quantifying mouse cognitive function. In the present study, we used the touchscreen paradigm to assess the effects of the mdx mutation on visual discrimination learning, serial reversal learning, and extinction learning. To enable measuring task-dependent learning and memory processes while holding demands on sensory-driven information processing constant, we developed equally salient visual stimuli and used them on all experimental stages. Acquisition of the initial pairwise visual discrimination was facilitated in mdx mice relative to wildtype littermates; this effect was not explained by genotypic differences in impulsivity, motivation, or motor deficits. The mdx mutation had no effect on serial reversal or extinction learning. Together, findings from this study and previous studies suggest that mdx effects on cognitive function are task-specific and may be influenced by discrimination type (spatial, visual), reward type (food, escape from a non-preferred environment), sex, and genetic background.
topic Duchenne muscular dystrophy
dystrophin
C57BL/10ScSn-Dmdmdx
operant conditioning
touchscreen
behavioral flexibility
url https://www.frontiersin.org/article/10.3389/fnbeh.2019.00200/full
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